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Quality Control Associate Iii Jobs in California

Excellent employment opportunity for a QC Associate III in the Fremont, CA area. * Performs sampling/testing/inspection of raw materials, conducts lab investigations, and reports aberrant results to ...

QC Associate

Pico Rivera, CA · On-site

$16 - $18/hr

We are seeking a QC Associate to join our team! You will conduct tests to determine the quality of materials and finished products as well as identify areas of improvement to increase efficiency.

We are seeking a QC Associate to join our team! You will conduct tests to determine the quality of materials and finished products as well as identify areas of improvement to increase efficiency.

The Quality Control Associate is responsible for inspecting all food products in the warehouse and discerning whether or not they meet our high standards of quality. The Quality Control Associate ...

The Quality Control Associate is responsible for inspecting all food products in the warehouse and discerning whether or not they meet our high standards of quality. The Quality Control Associate ...

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he Quality Control Associate plays a critical role within the Quality Team, performing routine quality checks on vitamin gummies, tablets, capsules, powders, and IV products . This position focuses ...

The company is looking for a Sr. QC Associate to join the team. This is an amazing opportunity to ... Contract Duration: 3 months (Likely to extend) * Schedule: Monday-Friday, 8:00 AM-5:00 PM * Hours ...

QC Associate II

Fremont, CA · On-site

$30 - $33/hr

Pay Rate Low: 30 | Pay Rate High: 33 QC Associate II We are partnering with a multi-product ... The ideal candidate brings 3-5 years of relevant industry experience, hands-on analytical ...

Job Summary BioLegend has an immediate opening for a Quality Control Associate that will be responsible for testing products such as antibodies and proteins in the following application(s): flow ...

Regularly exercises discretion and in performing duties directly related to the general operation of product quality control. RESPONSIBILITIES Provide technical, customer relations, and personnel ...

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Quality Control Associate

Stockton, CA · On-site

$18.50 - $20/hr

Use Verified by QC · Check insulated glass department log twice daily. Verified by QC · Check finished products and logs twice daily. · Run a 15-minute sill water test and a weep drainage test at ...

Excellent employment opportunity for a QC Associate IV in the Fremont, CA area. * Reviews raw material lot packages and releases RM lots for GMP manufacturing use. * Ensures lot release timelines ...

Quality Control Associate

Union City, CA · On-site

$21.88 - $32.84/hr

Regularly exercises discretion and in performing duties directly related to the general operation of product quality control. RESPONSIBILITIES Provide technical, customer relations, and personnel ...

Join Lonza in Vacaville, CA as a Quality Control(QC) Associate I. You will be a team member of the Quality Control department to support production of in-process, drug substance, drug product, raw ...

Join Lonza in Vacaville, CA as a Quality Control(QC) Associate I. You will be a team member of the Quality Control department to support production of in-process, drug substance, drug product, raw ...

QC Associate II

Fremont, CA · On-site

$28 - $33/hr

Pay Range: $28.23hr - $33.23hr Requirement/Must Have: * 3-5 years of industry experience GMP ... associates on operations upon completion of trainer qualification. * Represents QC operations on ...

Cell Culture & QC Associate The Cell Culture & QC Associate supports a critical technology transfer and biomass scale-up project by performing hands-on mammalian cell culture and microbiological ...

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Quality Control Associate Iii information

What does a Quality Control Associate III do?

A Quality Control Associate III is responsible for performing advanced quality control testing and analysis to ensure products meet established standards and regulatory requirements. They typically oversee and mentor junior team members, review and interpret test results, troubleshoot issues, and help develop or refine quality control procedures. This role often involves working in laboratory settings, documenting findings, and collaborating with production and quality assurance teams to maintain high product quality.

What are the key skills and qualifications needed to thrive as a Quality Control Associate III, and why are they important?

To thrive as a Quality Control Associate III, you typically need a strong background in biology, chemistry, or a related field, along with experience in laboratory testing and quality assurance processes. Familiarity with technical tools such as HPLC, GC, LIMS, and compliance with GMP/GLP guidelines, as well as certifications like ASQ, are commonly required. Attention to detail, problem-solving, and effective communication are crucial soft skills for identifying issues and collaborating with cross-functional teams. These skills and qualifications ensure accurate testing, regulatory compliance, and the delivery of high-quality products in regulated industries.

What are some common challenges faced by a Quality Control Associate III, and how can they be addressed?

Quality Control Associate III professionals often encounter challenges such as managing tight deadlines for testing, adapting to evolving regulatory requirements, and troubleshooting unexpected deviations in product quality. Addressing these challenges requires strong organizational skills, a thorough understanding of compliance standards, and proactive communication with cross-functional teams like manufacturing and R&D. Leveraging robust documentation practices and continually updating knowledge through training can also help ensure accuracy and efficiency in quality control processes.

What is the difference between Quality Control Associate Iii vs Quality Control Associate Ii?

AspectQuality Control Associate IiiQuality Control Associate Ii
Required CredentialsTypically requires a bachelor's degree in a related field and relevant certificationsUsually requires an associate degree or equivalent experience, with some certifications preferred
Work EnvironmentLaboratory and manufacturing settings, performing complex testing and analysisSimilar environments but with more routine testing and data collection
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing industries for quality assuranceCommonly found in similar industries, supporting quality control processes

The main difference between Quality Control Associate Iii and Quality Control Associate Ii lies in experience, responsibilities, and required credentials. The Associate Iii typically handles more complex testing, requires higher education or certifications, and may supervise or mentor lower-level associates. The Associate Ii performs routine testing and data collection, supporting overall quality assurance efforts.

What cities in California are hiring for Quality Control Associate Iii jobs?

Cities in California with the most Quality Control Associate Iii job openings:

Quality Control Associate III, Sample Management

San Diego, CA • On-site

Capricor Therapeutics, Inc.
Biotechnology Research and Development • 11 - 50 employees

$80 - $100/hr

Other

Posted 7 days ago


Job description

The Quality Control Associate III, Sample Management is responsible for the receipt, tracking, storage, distribution, and disposal of samples in a controlled laboratory or regulated environment. This role ensures sample integrity, accurate documentation, and compliance with applicable regulatory and quality standards.

Responsibilities
  • Receive, log, label, and track incoming samples using a laboratory information management system (LIMS) or equivalent tracking system
  • Verify sample documentation for accuracy, completeness, and compliance with protocols
  • Maintain proper storage conditions (e.g., temperature‑controlled environments such as refrigerators, freezers, and ambient storage)
  • Monitor and document storage conditions, including temperature logs and alarm responses
  • Coordinate sample distribution (i.e., in‑house, release, and stability) to internal departments or external laboratories
  • Ensure chain‑of‑custody documentation is accurate and maintained
  • Perform inventory management, including reconciliation and periodic audits
  • Dispose of samples according to safety, regulatory, and company procedures
  • Investigate and document sample discrepancies, deviations, or nonconformances
  • Support laboratory operations by preparing materials as needed
  • Maintain clean, organized, and compliant storage areas
Required Qualifications (Must‑Haves)
  • Bachelor’s degree in Biology, Chemistry, Microbiology, or a related scientific field (or equivalent experience)
  • 3–5 years of experience in a laboratory, sample management, or regulated environment
  • Familiarity with LIMS or electronic tracking systems
  • Knowledge of GMP/GLP regulations
Skills and Competencies
  • Strong attention to detail and organizational skills
  • Ability to manage multiple priorities and meet deadlines
  • Good documentation practices (GDP) knowledge
  • Strong communication and teamwork skills
  • Problem‑solving and critical thinking abilities
Work Environment & Physical Requirements
  • Ability to sit or stand for extended periods and move throughout the facility
  • Ability to gown and enter classified areas when required
  • Ability to lift and carry up to 40 lbs as needed

$75,000 - $95,000 a year

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